| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48841469-48841697 | Common:2; Rare:25 | ||||
| chr17:48944740-48944901 | Common:1; Rare:61 | ||||
| chr17:48997125-48997477 | Rare:67 | ||||
| chr17:49210228-49210455 | Common:2; Rare:35 | ||||
| chr17:49210581-49210718 | Rare:20 | ||||
| chr17:49230740-49230861 | Common:2; Rare:37 | ||||
| chr17:49414833-49415132 | Common:2; Rare:71 | ||||
| chr17:49788576-49788759 | Common:1; Rare:61 | ||||
| chr17:50095181-50095449 | Common:2; Rare:81 | ||||
| chr17:50165809-50165941 | Rare:22 | ||||
| chr17:50165961-50166071 | Common:1; Rare:40; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:50188527-50189017 | Rare:125; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr17:50189167-50189683 | Rare:117; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:50192818-50193043 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:50194129-50194377 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):3 |